ClinVar Miner

Variants studied for neural tube defects, folate-sensitive

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
43 110 36 11 3 199

Gene and significance breakdown #

Total genes and gene combinations: 5
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
MTHFR 31 62 15 5 1 111
MTRR 12 48 6 2 1 68
C1orf167, MTHFR 0 0 7 1 1 9
MTR 0 0 4 3 0 7
MTHFD1 0 0 4 0 0 4

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Baylor Genetics 41 107 4 0 0 152
Fulgent Genetics, Fulgent Genetics 6 6 16 9 1 38
Illumina Laboratory Services, Illumina 0 0 14 1 1 16
Mendelics 1 0 0 1 1 3
Juno Genomics, Hangzhou Juno Genomics, Inc 0 2 1 0 0 3
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 1 0 0 1
iDNA Genomics 0 0 0 1 0 1

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